scholarly journals Modeling the properties of Kukersite shale gasoline

2021 ◽  
Author(s):  
Parsa Mozaffari ◽  
zachariah Steven baird ◽  
oliver järvik

Based on new experimental data for Kukersite shale oil, it is now possible to develop a property prediction model for the gasoline fraction of shale oil. Such a model was created based on estimation of the composition along with experimental boiling point and density data. First, correlations were developed to estimate the composition of a Kukersite shale gasoline sample based on the boiling point and density of narrow fractions. The estimated composition was then used with the PC-SAFT equation of state to calculate the properties of shale gasoline. To do so, correlations were developed to predict the PC-SAFT parameters of the various classes of compounds present in Kukersite shale gasoline. The utility of this model was shown by predicting the vapor pressure of various portions of the shale gasoline.

2018 ◽  
Vol 40 (4) ◽  
pp. 387-395
Author(s):  
Phan Thi Thu Huong ◽  
Lai Ngoc Anh

This paper presents the study on the determination of the thermodynamic properties of Cis-1,3,3,3-tetrafluoropropene (R1234ze(Z)) with the BACKONE equation of state. The BACKONE's characteristic temperature T0, characteristic density ρ0, anisotropy factor α, and reduce quarupole moment Q*2 were found by fitting the BACKONE EOS to experimental data of vapor pressure and saturated liquid density. All thermodynamic properties such as vapor pressure, pressure in gaseous phase, saturated liquid density, and liquid density can be determined easily from the found molecular characteristic properties. Thermodynamic properties of the R1234ze(Z) were evaluated with available experimental data. Average absolute deviations between calculated vapor pressure data and experimental data were 0.43%. Average absolute deviations between calculated saturated liquid density data and experimental data were 0.43%. In the prediction of the thermodynamic properties, average absolute deviations between calculated liquid density data and experimental data were 0.68% and average absolute deviations between calculated gas density data and experimental data were 1.6%.


1977 ◽  
Vol 17 (04) ◽  
pp. 281-286 ◽  
Author(s):  
J.N. Robinson ◽  
E. Wichert ◽  
R.G. Moore ◽  
R.A. Heideman

Abstract Equilibrium water contents of sour natural gases are predicted using the Soave modification of the Redlich-Kwong equation of state. Calculated results are compared with published experimental data and with 180 field observations that were collected from the natural gas industry of western Canada and France. Computer-generated curves are provided to enable field calculation of the equilibrium water content of sour natural gases over a greater range of conditions than is possible with other methods. Introduction Natural gases containing significant quantities of acid gas are encountered frequently in western Canada. Estimates of the water content of these sour gases are required for the design of plant and pipeline facilities. This paper describes an pipeline facilities. This paper describes an equation-of-state method for predicting water content and presents a summary of field data gathered for testing the model. Three methods are currently available for estimating the water content of sour natural gases. In the procedure outlined by the Gas Processors Suppliers Assn. (GPSA), the estimated water content of a sour gas is a molar average of the solubility of water in the hydrocarbons, hydrogen sulfide, and carbon dioxide. The water-content curves for H2S and CO2 are based on experimental data for the binary mixtures H2O-H2S and H2O-CO2, respectively. Both these binaries display liquid-liquid equilibria at temperatures and pressures common in processing applications, and the water content read for the acid gas components often corresponds to the solubility of water in a nonaqueous liquid phase rather than in a vapor phase. In general, the predicted water content of sour natural gases is predicted water content of sour natural gases is high when based on these experimental curves. Maddox presents a method similar to the GPSA procedure. The difference is that the effect of procedure. The difference is that the effect of liquid-liquid separation has been removed from the H2O-CO2 and H2O-H2S binary data by smoothing. Campbell is credited with generating the curves, which terminate at 204 atm (3,000 Psi). Use of the modified curves in the molar averaging method can be expected to result in low estimates of the water content at elevated pressures. A semi-empirical correlation based on calculated mixture properties was developed by Sharma and Campbell. This method yields satisfactory estimates of water content for sour gases having total acid gas concentrations less than 15 percent, at temperatures between 300 (80 deg. F) and 344 K (160 deg. F), and at pressures less than 136 atm (2,000 psi). The major limitation of these three methods is that there is no basis for extrapolation to high acid gas concentrations or to more extreme conditions of temperature and pressure. When an equation of state is used to estimate the water content, as we have done in this paper there is, in principle, no limitation on the range of conditions that can be considered. It has been demonstrated previously that an equation of state can be used to describe waterhydrocarbon systems and the two binary pairs H2O-CO2 and H2O-H2S. In this paper, the Soave modification of the Redlich-Kwong equation has been used to calculate the water content of sour natural gases. Comparison is made with 180 field measurements taken in western Canada and in France. THE EQUATION OF STATE Soave presented a modification of the Redlich-Kwong equation in which the coefficient a was correlated against reduced temperature and acentricity so as to match vapor-pressure data of pure components. We have used this equation to pure components. We have used this equation to describe both the liquid and vapor phases. Evelein et al. found that the vapor pressure of water was not predicted with satisfactory accuracy by the Soave correlation, and presented alternative values of a for water. SPEJ P. 281


2008 ◽  
Vol 59 (5) ◽  
Author(s):  
Viorel Feroiu ◽  
Dan Geana ◽  
Catinca Secuianu

Vapour � liquid equilibrium, thermodynamic and volumetric properties were predicted for three pure hydrofluorocarbons: difluoromethane (R32), pentafluoroethane (R125) and 1,1,1,2 � tetrafluoroethane (R134a) as well as for binary and ternary mixtures of these refrigerants. Three cubic equations of state GEOS3C, SRK (Soave � Redlich � Kwong) and PR (Peng � Robinson) were used. A wide comparison with literature experimental data was made. For the refrigerant mixtures, classical van der Waals mixing rules without interaction parameters were used. The GEOS3C equation, with three parameters estimated by matching several points on the saturation curve (vapor pressure and corresponding liquid volumes), compares favorably to other equations in literature, being simple enough for applications.


1983 ◽  
Vol 48 (9) ◽  
pp. 2446-2453 ◽  
Author(s):  
Jan Linek

Isothermal vapour-liquid equilibrium data at 65, 73 and 80 °C and isobaric ones at 101.3 kPa were measured in the tetrachloromethane-sec-butyl alcohol system. A modified circulation still of the Gillespie type was used for the measurements. Under the conditions of measurement, the system exhibits positive deviations from Raoult's law and minimum boiling-point azeotropes. The experimental data were fitted to a number of correlation equations, the most suitable being the Wilson equation.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ilyas Al-Kindi ◽  
Tayfun Babadagli

AbstractThe thermodynamics of fluids in confined (capillary) media is different from the bulk conditions due to the effects of the surface tension, wettability, and pore radius as described by the classical Kelvin equation. This study provides experimental data showing the deviation of propane vapour pressures in capillary media from the bulk conditions. Comparisons were also made with the vapour pressures calculated by the Peng–Robinson equation-of-state (PR-EOS). While the propane vapour pressures measured using synthetic capillary medium models (Hele–Shaw cells and microfluidic chips) were comparable with those measured at bulk conditions, the measured vapour pressures in the rock samples (sandstone, limestone, tight sandstone, and shale) were 15% (on average) less than those modelled by PR-EOS.


Energies ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1315
Author(s):  
Jingwei Huang ◽  
Hongsheng Wang

Confined phase behavior plays a critical role in predicting production from shale reservoirs. In this work, a pseudo-potential lattice Boltzmann method is applied to directly model the phase equilibrium of fluids in nanopores. First, vapor-liquid equilibrium is simulated by capturing the sudden jump on simulated adsorption isotherms in a capillary tube. In addition, effect of pore size distribution on phase equilibrium is evaluated by using a bundle of capillary tubes of various sizes. Simulated coexistence curves indicate that an effective pore size can be used to account for the effects of pore size distribution on confined phase behavior. With simulated coexistence curves from pore-scale simulation, a modified equation of state is built and applied to model the thermodynamic phase diagram of shale oil. Shifted critical properties and suppressed bubble points are observed when effects of confinement is considered. The compositional simulation shows that both predicted oil and gas production will be higher if the modified equation of state is implemented. Results are compared with those using methods of capillary pressure and critical shift.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hua Shu ◽  
Jiangtao Li ◽  
Yucheng Tu ◽  
Junjian Ye ◽  
Junyue Wang ◽  
...  

AbstractThe sound velocities of water in the Hugoniot states are investigated by laser shock compression of precompressed water in a diamond anvil cell. The obtained sound velocities in the off-Hugoniot region of liquid water at precompressed conditions are used to test the predictions of quantum molecular dynamics (QMD) simulations and the SESAME equation-of-state (EOS) library. It is found that the prediction of QMD simulations agrees with the experimental data while the prediction of SESAME EOS library underestimates the sound velocities probably due to its improper accounting for the ionization processes.


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